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T10630BuChE-IN-TM-10
BuChE-IN-TM-10 is a potent butyrylcholinesterase (BuChE) inhibitor, with an IC50 of 8.9 nM. BuChE inhibitor 1 inhibits and disaggregates self-induced Aβ aggregation, exhibiting potent antioxidant activity and good blood-brain barrier (BBB) penetration. Has potential to treat Alzheimer’s disease.
价 格：￥电议型 号：T10630产 地：中国大陆
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T40024Pomalidomide-PEG1-CO2H
Pomalidomide-PEG1-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker.
价 格：￥电议型 号：T40024产 地：中国大陆
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T94215-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid5(5Flu
5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid is a chemical compound.
价 格：￥电议型 号：T9421产 地：中国大陆
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TQ0105CAY10650acanthamoeba,inhibit,CAY 10650,PGE2,CAY10650,lipid droplets,neutrophils,keratitis,mannose-in
CAY10650 is an effective inhibitor of cytosolic phospholipase A2α (cPLA2α, IC50: 12 nM).
价 格：￥电议型 号：TQ0105产 地：中国大陆
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T8561Apcinligase,pocket,anaphase-promoting,Apcin,recognition,complex,Inhibitor,Cdc20,Anaphase promoting c
Apcin is a potent and competitive inhibitor of anaphase-promoting complex/cyclosome (APC/C(Cdc20)) E3 ligase activity. Apcin competitively inhibits APC/C-dependent ubiquitylation by binding to Cdc20 and preventing substrate recognition. It acts by blocking mitotic exit and being synergistically amplified by co-addition of Ts-Arg-OMe.
价 格：￥电议型 号：T8561产 地：中国大陆
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TP2310Autocamtide-2-related inhibitory peptideCalmodulin-dependent protein kinases,Autocamtide2related inh
Autocamtide-2-related inhibitory peptide is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.
价 格：￥电议型 号：TP2310产 地：中国大陆
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T6659SB 415286inhibit,GSK-3,Inhibitor,Glycogen synthase kinase 3,Glycogen synthase kinase-3,Apoptosis,SB-
SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β.
价 格：￥电议型 号：T6659产 地：中国大陆
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T9887ethyl 1-[(4-cyanobenzyl)oxy]-2-(3-cyanophenyl)-4-methyl-1H-imidazole-5-carboxylateethyl 1[(4cyanoben
ethyl 1-[(4-cyanobenzyl)oxy]-2-(3-cyanophenyl)-4-methyl-1H-imidazole-5-carboxylate is a platelet aggregation inhibitor.
价 格：￥电议型 号：T9887产 地：中国大陆
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T7753Thalidomide-O-COOHinhibit,Ligands for E3 Ligase,ThalidomideOCOOH,Inhibitor,Thalidomide O COOH,Cerebl
Thalidomide-O-COOH is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTACs.
价 格：￥电议型 号：T7753产 地：中国大陆
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T8816NAE-IN-M22NAEINM22,cancer,Inhibitor,NAE-IN-M-22,NAE,NEDD8,NAE IN M22,enzyme,activating,inhibit,tumor
NAE-IN-M22 is a selective, potent and reversible inhibitor of NEDD8 activating enzyme (NAE). NAE-IN-M22 inhibits multiple cancer cell lines and induces apoptosis in A549 cells. NAE-IN-M22 also can inhibit tumor growth in vivo.
价 格：￥电议型 号：T8816产 地：中国大陆
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T12483Piperidine-MO-1Piperidine MO 1,PiperidineMO1
Piperidine-MO-1 is a dopamine receptor modulator, with an ED50 of 68 μmol/kg on increase of DOPAC in the rat striatum (WO/2005/121087A1, compound example 2).
价 格：￥电议型 号：T12483产 地：中国大陆
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T9389Thalidomide-PEG4-PropargylE3 Ligase Ligand-Linker Conjugates,Thalidomide-PEG-4-Propargyl,inhibit,Inh
Thalidomide-PEG4-Propargyl is a synthetic E3 ligase ligand-linker conjugate containing a Thalidomide-based cereblon ligand and a linker which can be used in PROTAC technology[1].
价 格：￥电议型 号：T9389产 地：中国大陆
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TP2493Tripeptide-10 citrulline AcetateTripeptide10 citrulline Acetate,Tripeptide 10 citrulline Acetate
Tripeptide-10 citrulline Acetate has been shown to have anti-wrinkle and cosmetic effects.
价 格：￥电议型 号：TP2493产 地：中国大陆
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TP1212N-Boc-Phe-Leu-Phe-Leu-PheN Boc Phe Leu Phe Leu Phe,inhibit,Inhibitor,NBocPheLeuPheLeuPhe
N-Boc-Phe-Leu-Phe-Leu-Phe (Boc-FLFLF) is a formyl peptide receptor 1 (FPR1) antagonist, which increases pain effects and inhibits antinociceptive activity of annexin. Boc-Phe-Leu-Phe-Leu-Phe is used extensively in FPR research.
价 格：￥电议型 号：TP1212产 地：中国大陆
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TN70872,5-dimethoxycyclohexa-2,5-diene-1,4-dio2,5dimethoxycyclohexa2,5diene1,4dio,2,5 dimethoxycyclohexa 2
2,5-dimethoxycyclohexa-2,5-diene-1,4-dio is a natural product. The redox cycle of 2,5-dimethoxybenzoquinone is a source of reducing equivalent for the regeneration of Fe2+ and H2O2 in brown rot fungal decay of wood.
价 格：￥电议型 号：TN7087产 地：中国大陆
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T74612,4-Diamino-6-hydroxypyrimidinecyclohydrolase-I,VCAM-1,inhibit,GTP,NO Synthase,2,4Diamino6hydroxypyr
2,4-Diamino-6-hydroxypyrimidine (DAHP) is a selective, specific inhibitor of GTP cyclohydrolase I, the rate limiting step for de novo pterin synthesis
价 格：￥电议型 号：T7461产 地：中国大陆
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T7513Protease-Activated Receptor-2, amideProteaseActivated Receptor2, amide,Protease Activated Receptor (
Protease-Activated Receptor-2, amide is an agonist of PAR2 (IC50 : 10.4 M)
价 格：￥电议型 号：T7513产 地：中国大陆
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TN2126Quercetin-3-O-glucose-6’’-acetateQuercetin3Oglucose6’’acetate,Quercetin 3 O glucose 6’’ acetate
Quercetin-3-O-glucose-6´´-acetate is an inhibitor of NADPH oxidase. Quercetin-3-O-glucose-6´´-acetate has antioxidant activities.
价 格：￥电议型 号：TN2126产 地：中国大陆
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TQ0033ZegocractinInhibitor,inhibit,Calcium release-activated channels,Ca2+ release-activated Ca2+ channels
CM4620 is a calcium-release activated calcium-channel (CRAC channel) inhibitor.
价 格：￥电议型 号：TQ0033产 地：中国大陆
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T6148CX-6258 hydrochlorideCX6258 hydrochloride,Pim,CX6258,CX-6258,Pim kinases,4E-BP1,CX 6258 hydrochlorid
CX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
价 格：￥电议型 号：T6148产 地：中国大陆
